Garnier Skin Naturals Lift SPF 15 Day by L'Oreal USA Products Inc Drug Facts

Garnier Skin Naturals Lift SPF 15 Day by

Drug Labeling and Warnings

Garnier Skin Naturals Lift SPF 15 Day by is a Otc medication manufactured, distributed, or labeled by L'Oreal USA Products Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

GARNIER SKIN NATURALS LIFT SPF 15 DAY- ensulizole and octinoxate cream 
L'Oreal USA Products Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredients

Ensulizole 1.7%; Octinoxate 7.5%

Warnings

For external use only

When using this product

AVOID CONTACT WITH THE EYES. 

Stop use and consult a doctor if

SIGNS OF IRRITATION DEVELOPS OR INCREASES.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Apply every morning before sun exposure with light circular movements, moving from the center of your face outwards, and from the base to the top of your neck.

Inactive ingredients

water, dimethicone, glycerin, myristyl myristate, stearic acid, triethanolamine, palmitic acid, ammonium polyacryloyldimethyl taurate, ci 77891, peg-100 stearate, glyceryl stearate, stearyl alcohol, cera alba, cetyl alcohol, caprylyl glycol, paraffin, peg-20 stearate, argania spinosa, retinyl linoleate, acrylates copolymer, disodium edta, phenoxyethanol, hydrolyzed rice protein, glycine soja oil, carbomer, cera carnauba, tocopherol, capryloyl salicylic acid, alumina, sodium cocoyl glutamate, zingiber officinale root extract, methylparaben, ethylparaben, benzyl alcohol, linalool, citral, limonene, coumarin

GARNIER SKIN NATURALS LIFT SPF 15 DAY 
ensulizole and octinoxate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49967-671
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Ensulizole (UNII: 9YQ9DI1W42) (Ensulizole - UNII:9YQ9DI1W42)	Ensulizole	17 mg  in 1 mL
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	75 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCERIN (UNII: PDC6A3C0OX)
MYRISTYL MYRISTATE (UNII: 4042ZC00DY)
STEARIC ACID (UNII: 4ELV7Z65AP)
PALMITIC ACID (UNII: 2V16EO95H1)
PEG-100 STEARATE (UNII: YD01N1999R)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
CETYL ALCOHOL (UNII: 936JST6JCN)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PARAFFIN (UNII: I9O0E3H2ZE)
PEG-20 STEARATE (UNII: NBX892EA57)
RETINYL LINOLEATE (UNII: 61911N8D6W)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TOCOPHEROL (UNII: R0ZB2556P8)
CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4)
SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
METHYLPARABEN (UNII: A2I8C7HI9T)
ETHYLPARABEN (UNII: 14255EXE39)
BENZYL ALCOHOL (UNII: LKG8494WBH)
CITRAL (UNII: T7EU0O9VPP)
COUMARIN (UNII: A4VZ22K1WT)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49967-671-01	1 in 1 CARTON	07/01/2011	06/23/2017
1		50 mL in 1 JAR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	07/01/2011	06/23/2017

Labeler - L'Oreal USA Products Inc (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
L'Oreal USA Products Inc		624244349	manufacture(49967-671)

Revised: 1/2020

Document Id: 01f26c08-ad9b-450f-aa36-ed18fd9e8baf

34390-5

Set id: 9470c7d8-281b-4e24-912f-d88aced33ac5

Version: 4

Effective Time: 20200117

 

L'Oreal USA Products Inc